Search Results: 1 unique variant retrieved.
Terms with a '*' next to them are explained on the Help Page .
c.574G>C
p.Gly192Arg (Legacy AA No. 152)
Variant Type:
Point
Domain:
Activation peptide
Location:
Exon 6
Variant Effect:
Missense
Codon Change:
G>C
No. of Patients Reported:
0
Phenotype:
U
Allele Count *:
1
Allele Number *:
248970
Allele Frequency *:
0.000004